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First Aid Antiseptic

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This product has been discontinued

Active ingredients
  • Lidocaine Hydrochloride 25 mg/1 mL
  • Benzalkonium Chloride 1.3 mg/1 mL
Other brand names
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2013
Label revision date
July 10, 2018
Active ingredients
  • Lidocaine Hydrochloride 25 mg/1 mL
  • Benzalkonium Chloride 1.3 mg/1 mL
Other brand names
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2013
Label revision date
July 10, 2018
Manufacturer
Premier Value
Registration number
part348
NDC root
68016-269

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Drug Overview

You can use this medication as a first aid treatment to help prevent bacterial contamination or skin infections. It is also effective for providing temporary relief from pain and itching associated with minor cuts, scrapes, burns, sunburn, and skin irritations. This makes it a helpful option for managing minor skin injuries and discomfort.

Uses

You can use this product for first aid to help prevent bacterial contamination or skin infections. It’s also effective for providing temporary relief from pain and itching caused by minor cuts, scrapes, burns, sunburn, and other skin irritations. Whether you’re dealing with a small injury or just some discomfort on your skin, this product can help you feel more comfortable and protected.

Dosage and Administration

To use this medication, start by cleaning the affected area thoroughly. Once it's clean, apply a small amount of the medication directly to the area. You can do this 1 to 3 times a day, depending on your needs. If you prefer, you can cover the area with a sterile bandage after the medication has dried.

If you are using this medication for a child under 2 years old, it's important to consult a physician (doctor) before applying it. This ensures that the treatment is safe and appropriate for their age.

What to Avoid

It's important to use this medication safely to avoid potential issues. You should never apply it in or near your eyes, as this can cause irritation or harm. Additionally, avoid using it over large areas of your body or in large quantities, as this may lead to unwanted effects. Lastly, do not apply it to raw surfaces or blistered areas, as this can exacerbate irritation or lead to complications. Always follow these guidelines to ensure your safety and the effectiveness of the treatment.

Side Effects

When using this product, it's important to remember that it is for external use only. Avoid applying it near your eyes, over large areas of your body, or on raw or blistered skin. If you have deep or puncture wounds, animal bites, or serious burns, consult your doctor before use.

You should stop using the product and seek medical advice if your condition worsens, if symptoms last more than 7 days, or if they improve and then return within a few days. Keep this product out of reach of children, and if swallowed, seek medical help or contact a Poison Control Center immediately.

Warnings and Precautions

This product is for external use only. Before using it, please consult your doctor if you have deep or puncture wounds, animal bites, or serious burns. While using the product, avoid contact with your eyes, and do not apply it over large areas of your body or in large amounts. It should also not be used on raw surfaces or blistered areas.

If your condition worsens, or if your symptoms last more than 7 days or improve and then return within a few days, stop using the product and contact your doctor. Additionally, if the product is swallowed, seek emergency medical help or contact a Poison Control Center immediately.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, don’t wait—get help right away. Remember, acting quickly can make a significant difference in the outcome.

Pregnancy Use

Currently, there is no available information about the use of this medication during pregnancy, including any safety concerns, necessary dosage adjustments, or specific precautions you should take. If you are pregnant or planning to become pregnant, it is essential to discuss any medications with your healthcare provider to ensure the safety of both you and your baby. Always prioritize open communication with your doctor regarding any potential risks associated with medications during pregnancy.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of this product while nursing. Additionally, there are no statements about the product being excreted in breast milk or any associated risks for your infant. This means that, based on current information, you can use this product without concern for its effects on your milk production or your baby's health.

Pediatric Use

If your child is under 2 years old, it's important to consult a physician (doctor) before using this medication. For children aged 2 years and older, you should first clean the affected area. Then, apply a small amount of the medication to the area 1 to 3 times a day. If needed, you can cover it with a sterile bandage, but make sure the area is dry before doing so. Always follow these guidelines to ensure your child's safety and well-being.

Geriatric Use

When it comes to using this medication in older adults, there is no specific information available about dosage adjustments, safety concerns, or special precautions. This means that if you or a loved one is an older adult considering this medication, it’s important to consult with a healthcare provider. They can help determine the best approach based on individual health needs and any other medications being taken. Always prioritize open communication with your healthcare team to ensure safe and effective treatment.

Renal Impairment

If you have kidney problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or safety considerations for your condition. This means that there are no tailored guidelines for how this medication may affect you if you have renal impairment (kidney issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your health situation. They can help monitor your kidney function and make any necessary adjustments to your treatment plan.

Hepatic Impairment

If you have liver problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or precautions for your condition. This means that there are no tailored guidelines for how this medication may affect you if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to discuss any concerns regarding your liver health and how it may relate to your treatment. They can help ensure that you receive the safest and most effective care.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that the medication may not have known conflicts with other drugs or tests. However, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective based on your unique health situation.

Always discuss any new medications or tests with your healthcare provider to avoid potential issues and to get the best care possible. Your health and safety should always come first.

Storage and Handling

To ensure the safety and effectiveness of your product, it's important to store it in a cool, dry place. Avoid exposing it to excessive heat, as this can compromise its quality. When handling the product, make sure to follow any specific instructions provided to maintain its integrity and safety.

If you have any components that come with the product, be sure to understand their role in its use and handle them with care. Always dispose of any materials according to local regulations to ensure safety for yourself and the environment.

Additional Information

No further information is available.

FAQ

What is the primary use of this product?

This product is used as first aid to help prevent bacterial contamination or skin infection and to provide temporary relief of pain and itching associated with minor cuts, scrapes, burns, sunburn, and skin irritations.

How should I use this product?

For adults and children 2 years and older, clean the affected area and apply a small amount 1-3 times daily. It may be covered with a sterile bandage after drying.

What should I do if I have children under 2 years?

Consult a physician before using this product on children under 2 years.

Are there any warnings I should be aware of?

This product is for external use only. Do not use it in or near the eyes, over large areas of the body, or on raw surfaces or blistered areas.

What should I do if my condition worsens?

Stop using the product and ask a doctor if your condition worsens or if symptoms persist for more than 7 days.

What should I do if I accidentally swallow this product?

If swallowed, get medical help or contact a Poison Control Center right away.

Can I use this product if I have deep or puncture wounds?

You should ask a doctor before using this product if you have deep or puncture wounds, animal bites, or serious burns.

Packaging Info

Below are the non-prescription pack sizes of First Aid Antiseptic (benzalkonium 0.13%, lidocaine hcl 2.5%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for First Aid Antiseptic.
Details

Drug Information (PDF)

This file contains official product information for First Aid Antiseptic, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

The drug is presented in the package label featuring a principal display panel. The effective date of the insert is July 10, 2018. Additionally, the insert includes a reference to an image, characterized as "image description," with a media type of image/jpeg and a reference value of "label.jpg."

Uses and Indications

This drug is indicated for first aid to help prevent bacterial contamination or skin infection. It provides temporary relief of pain and itching associated with minor cuts, scrapes, burns, sunburn, and skin irritations.

Limitations of Use: This drug is intended for external use only and should not be applied to deep wounds, animal bites, or serious burns.

Dosage and Administration

For adults and children aged 2 years and older, the affected area should be cleaned prior to application. A small amount of the medication should be applied to the area 1 to 3 times daily. If desired, the area may be covered with a sterile bandage after the medication has dried.

For children under 2 years of age, it is recommended to consult a physician before use.

Contraindications

Use of this product is contraindicated in the following situations:

Application in or near the eyes is prohibited due to the potential for irritation or damage to ocular tissues. Additionally, the product should not be applied over large areas of the body or in large quantities, as this may increase the risk of systemic absorption and adverse effects. Furthermore, application over raw surfaces or blistered areas is contraindicated to prevent exacerbation of irritation or potential infection.

Warnings and Precautions

For external use only.

Healthcare professionals should advise patients to consult a physician prior to use if they have deep or puncture wounds, animal bites, or serious burns. It is imperative to instruct patients on the proper application of this product. Specifically, it should not be used in or near the eyes, applied over large areas of the body, or used in large quantities. Additionally, the product must not be applied to raw surfaces or blistered areas to prevent adverse effects.

Patients should be informed to discontinue use and seek medical advice if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days.

In the event of accidental ingestion, immediate medical assistance should be sought, or the patient should contact a Poison Control Center without delay.

Side Effects

Patients using this product should be aware that it is intended for external use only. It is important to consult a healthcare professional prior to use if there are any deep or puncture wounds, animal bites, or serious burns present.

While using this product, patients should avoid contact with the eyes and refrain from applying it over large areas of the body or in excessive quantities. Additionally, it should not be applied to raw surfaces or blistered areas.

Patients are advised to discontinue use and seek medical advice if their condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days.

This product should be kept out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought or contact with a Poison Control Center should be made without delay.

Drug Interactions

No specific drug interactions have been identified in the available data. Additionally, there are no reported interactions between the drug and laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on the current information.

Packaging & NDC

Below are the non-prescription pack sizes of First Aid Antiseptic (benzalkonium 0.13%, lidocaine hcl 2.5%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for First Aid Antiseptic.
Details

Pediatric Use

Pediatric patients under 2 years of age should consult a physician prior to use. For children aged 2 years and older, the affected area should be cleaned before application. A small amount of the product may be applied to the area 1 to 3 times daily, and it may be covered with a sterile bandage after allowing it to dry.

Geriatric Use

There is no specific information regarding the use of this medication in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this medication to elderly patients, as individual responses may vary. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

There is currently no information available regarding the use of this drug during pregnancy, including safety concerns, dosage modifications, or any special precautions that should be taken. Healthcare professionals are advised to consider the lack of data when prescribing this medication to pregnant patients and to weigh the potential risks and benefits. Women of childbearing potential should be counseled on the absence of information related to pregnancy and encouraged to discuss any concerns with their healthcare provider.

Lactation

There are no specific warnings or recommendations regarding the use of this product by lactating mothers. Additionally, there are no statements concerning the potential for excretion in breast milk or any associated risks to breastfed infants during the use of this product.

Renal Impairment

Patients with renal impairment have no specific information regarding dosage adjustments, special monitoring, or safety considerations provided in the drug insert. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the lack of data necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in these patients to ensure safety and efficacy.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in clinical trials for this medication. Consequently, there is no available information regarding dosage adjustments, special monitoring requirements, or precautions for individuals with compromised liver function. It is recommended that healthcare providers exercise caution when prescribing this medication to patients with hepatic impairment, given the lack of data on its safety and efficacy in this population. Regular monitoring of liver function may be warranted based on clinical judgment.

Overdosage

In the event of an overdosage, immediate medical assistance is crucial. If the substance is swallowed, it is imperative to seek medical help or contact a Poison Control Center without delay.

Healthcare professionals should be aware that prompt intervention can significantly mitigate potential adverse effects associated with overdosage. Monitoring the patient for any symptoms that may arise is essential, as the specific manifestations of overdosage can vary depending on the substance involved.

Management procedures should include a thorough assessment of the patient's condition and the implementation of appropriate supportive care measures. It is advisable to follow established protocols for the management of overdosage, which may include decontamination, symptomatic treatment, and monitoring of vital signs.

In summary, swift action and adherence to recommended guidelines are critical in the management of overdosage cases to ensure patient safety and optimal outcomes.

Nonclinical Toxicology

No teratogenic or non-teratogenic effects have been reported in the available nonclinical studies. Additionally, there is no information regarding animal pharmacology and toxicology. The absence of data in these areas limits the understanding of the compound's potential effects in nonclinical settings.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion. In the event of swallowing the product, patients should seek medical help or contact a Poison Control Center immediately.

Patients should be instructed to discontinue use and consult a doctor if their condition worsens or if symptoms persist for more than 7 days. Additionally, if symptoms clear up and then recur within a few days, patients should also stop use and seek medical advice.

It is important to inform patients that this product should not be used in or near the eyes. They should be cautioned against applying the product over large areas of the body or in large quantities. Furthermore, patients should avoid applying the product over raw surfaces or blistered areas.

Healthcare providers should recommend that patients consult a doctor before using this product if they have deep or puncture wounds, animal bites, or serious burns.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product in a controlled environment, avoiding exposure to excessive heat to maintain its integrity and efficacy. Proper handling procedures should be followed to ensure optimal storage conditions are met.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for First Aid Antiseptic, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the FDA Structured Product Label (DailyMed) for First Aid Antiseptic, retrieved by a validated AI data-extraction workflow.

All FDA-listed dosage forms and strengths are shown in the Packaging & NDC Codes section above. Regulatory status appears in the Summary Information panel above and was verified in the FDA National Drug Code directory and the NSDE NDC Directory daily file.

Note: an automated daemon monitors NSDE checksums; when the record for this NDC changes, the new file is pulled instantly and this page is refreshed.

No human clinician has reviewed this version.

Learn more in our Editorial Policy

Last AI update:

Primary FDA sources:

Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.